Package 69292-265-01

Brand: pilocarpine hydrochloride

Generic: pilocarpine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69292-265-01
Digits Only 6929226501
Product NDC 69292-265
Description

100 TABLET, FILM COATED in 1 BOTTLE (69292-265-01)

Marketing

Marketing Status
Marketed Since 2022-07-26
Brand pilocarpine hydrochloride
Generic pilocarpine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e96671e2-f7a8-4d58-8b7f-35b9b7fab5a6", "openfda": {"upc": ["0369292265017"], "unii": ["0WW6D218XJ"], "rxcui": ["1000913"], "spl_set_id": ["a86a7b63-5f6a-4c10-9270-24c7b7d50437"], "manufacturer_name": ["AMICI PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69292-265-01)", "package_ndc": "69292-265-01", "marketing_start_date": "20220726"}], "brand_name": "Pilocarpine Hydrochloride", "product_id": "69292-265_e96671e2-f7a8-4d58-8b7f-35b9b7fab5a6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Agonists [MoA]", "Cholinergic Muscarinic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]"], "product_ndc": "69292-265", "generic_name": "PILOCARPINE HYDROCHLORIDE", "labeler_name": "AMICI PHARMACEUTICALS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pilocarpine Hydrochloride", "active_ingredients": [{"name": "PILOCARPINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076963", "marketing_category": "ANDA", "marketing_start_date": "20220726", "listing_expiration_date": "20261231"}